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- W2081053535 abstract "Dr Weiss makes the important point that when researchers design case–control studies of surveillance tests, it is important to use an interval equal to the DPP during which control screening is ascertained; otherwise, they will not count the right number of tests among controls. We agree that not knowing the detectable pre-clinical phase (DPP; in either the pre- or postdiagnosis context) is a limitation of these kinds of studies. One way to address this limitation is to assume that one can reasonably specify an interval after diagnosis during which a recurrence would not, theoretically, be detectable. If so, then in both cases and controls, one can use the end of that interval as the beginning of the (postdiagnosis) DPP." @default.
- W2081053535 created "2016-06-24" @default.
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- W2081053535 date "2011-01-01" @default.
- W2081053535 modified "2023-09-30" @default.
- W2081053535 title "Case–control studies of cancer surveillance procedures" @default.
- W2081053535 doi "https://doi.org/10.1016/j.jclinepi.2010.07.011" @default.
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